Compile Data Set for Download or QSAR
Found 79 with Last Name = 'kehraus' and Initial = 's'
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  150nMAssay Description:Displacement of [3H]CCPA from adenosine A1 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
TBA

Curated by ChEMBL
LigandPNGBDBM50382409(AMAUROMINE)copy SMILEScopy InChI
Affinity DataKi:  178nMAssay Description:Displacement of [3H]CP55940 from human recombinant CB1 receptor expressed in CHO cells after 2 hrs by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2PC33CXPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  210nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  240nMAssay Description:Displacement of [3H]R-PIA from adenosine A1 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  680nMAssay Description:Displacement of [3H]PSB-11 from human adenosine A3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  1.13E+3nMAssay Description:Displacement of [3H]-MSX-2 from Adenosine A2A receptor of rat striatal membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  1.18E+3nMAssay Description:Displacement of [3H]NECA from Adenosine A2A receptor of rat striatal membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataKi:  3.26E+3nMAssay Description:Displacement of [3H]CCPA from Adenosine A1 receptor of rat cortical membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataKi:  6.94E+3nMAssay Description:Displacement of [3H]PSB-11 from human adenosine A3 receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  8.20E+3nMAssay Description:Binding affinity towards human adenosine A2B receptor in VA13 fibroblasts as inhibition of adenylate cyclase at 10 uM; Less than 10% inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataKi:  9.45E+3nMAssay Description:Displacement of [3H]DPCPX from rat Adenosine A1 receptor of cortical membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataKi: >1.00E+4nMAssay Description:Displacement of [3H]PSB-298 from human adenosine A2B receptor expressed in HEK293 cells at 10 uMMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2b(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataKi:  1.39E+4nMAssay Description:Displacement of [3H]PSB-298 from human adenosine A2B receptor expressed in HEK293 cells at 10 uM; Less than 10% inhibitionMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A2a(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataKi:  1.71E+4nMAssay Description:Displacement of [3H]-MSX-2 from Adenosine A2A receptor of rat striatal membranesMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50094569(6-chloro-3,20-dioxo-1beta,2beta-dihydro-3'H-cyclop...)copy SMILEScopy InChI
Affinity DataIC50: 5nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes without GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50094569(6-chloro-3,20-dioxo-1beta,2beta-dihydro-3'H-cyclop...)copy SMILEScopy InChI
Affinity DataIC50: 125nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes with GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataIC50: 680nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes without GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAromatase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)copy SMILEScopy InChI
Affinity DataIC50: 800nMAssay Description:Inhibition of human recombinant aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X34XHFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM31768(CHEMBL295698 | Ketoconazole | Nizoral | Panfungol)copy SMILEScopy InChI
Affinity DataIC50: 900nMAssay Description:Inhibition of human recombinant aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
LigandPNGBDBM50577153(CHEMBL4873047)copy SMILES
Affinity DataIC50: 2.75E+3nMAssay Description:Inhibition of wild type GNAQ (unknown origin) expressed in CRISPR/Cas9 engineered HEK293 cellsMore data for this Ligand-Target Pair
Ligand InfoPC cidPC sid
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZK5MGSPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355307(CHEMBL1835012)copy SMILEScopy InChI
Affinity DataIC50: 3.01E+3nMAssay Description:Inhibition of human leukocyte elastase using MeOSuc-Ala-Ala-Pro-Val-para-nitroanilide chromogenic substrate after 10 mins spectrophotometricallyMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetAdenosine receptor A3(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataIC50: 6.70E+3nMAssay Description:Inhibition of forskolin-stimulated cAMP accumulation in chinese hamster ovary cell membranes expressing human adenosine A3 receptorMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetTYR_PHOSPHATASE_2 domain-containing protein(Mycobacterium tuberculosis)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50192335((2S,3S)-2-{3-[(3S,6S,9S,12S,15S)-3-benzyl-12-((S)-...)copy SMILEScopy InChI
Affinity DataIC50: 7.30E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis ptpbMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2708124PubMed
TargetTYR_PHOSPHATASE_2 domain-containing protein(Mycobacterium tuberculosis)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50192337((2S,3S)-2-(3-{(3S,6R,9S,12S,15S)-3-benzyl-9-isobut...)copy SMILEScopy InChI
Affinity DataIC50: 8.00E+3nMAssay Description:Inhibition of Mycobacterium tuberculosis ptpbMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2708124PubMed
TargetNeutrophil elastase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355305(CHEMBL1835010)copy SMILEScopy InChI
Affinity DataIC50: 9.28E+3nMAssay Description:Inhibition of human leukocyte elastase using MeOSuc-Ala-Ala-Pro-Val-para-nitroanilide chromogenic substrate after 10 mins spectrophotometricallyMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetN-arachidonyl glycine receptor(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448075(CHEMBL1258979)copy SMILEScopy InChI
Affinity DataIC50: 9.91E+3nMAssay Description:Inverse agonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 7.5 uM THC-mediated beta-arrestin recruitment after 90 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetN-arachidonyl glycine receptor(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448074(Emindole Sb)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 10 uM THC-mediated beta-arrestin recruitment after 90 mins by bet...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetG-protein coupled receptor 55(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448074(Emindole Sb)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetG-protein coupled receptor 55(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448076(CHEMBL3120632)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetG-protein coupled receptor 55(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448075(CHEMBL1258979)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetG-protein coupled receptor 55(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448073(CHEMBL3120631)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR55 expressed in CHO cells assessed as inhibition of LPI-mediated beta-arrestin recruitment after 90 mins by beta-gala...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetN-arachidonyl glycine receptor(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448073(CHEMBL3120631)copy SMILEScopy InChI
Affinity DataIC50: 1.00E+4nMAssay Description:Antagonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 10 uM THC-mediated beta-arrestin recruitment after 90 mins by bet...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50009685(9-METHYL-9H-PURIN-6-AMINE | 9-Methyl-9H-adenine | ...)copy SMILEScopy InChI
Affinity DataIC50: 1.25E+4nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes without GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetN-arachidonyl glycine receptor(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50448076(CHEMBL3120632)copy SMILEScopy InChI
Affinity DataIC50: 1.34E+4nMAssay Description:Inverse agonist activity at human GPR18 expressed in CHO cells assessed as inhibition of 7.5 uM THC-mediated beta-arrestin recruitment after 90 mins ...More data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2154JJZPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50009685(9-METHYL-9H-PURIN-6-AMINE | 9-Methyl-9H-adenine | ...)copy SMILEScopy InChI
Affinity DataIC50: 1.47E+4nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes with GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM22111((2R,3R,4S,5S)-2-(6-amino-9H-purin-9-yl)-5-[(methyl...)copy SMILEScopy InChI
Affinity DataIC50: 1.51E+4nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes with GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAromatase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50298231(CHEMBL576579 | Monodictyochromone B)copy SMILEScopy InChI
Affinity DataIC50: 1.65E+4nMAssay Description:Inhibition of human recombinant aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X34XHFPubMed
TargetNeutrophil elastase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355306(CHEMBL1835011)copy SMILEScopy InChI
Affinity DataIC50: 2.00E+4nMAssay Description:Inhibition of human leukocyte elastase using MeOSuc-Ala-Ala-Pro-Val-para-nitroanilide chromogenic substrate after 10 mins spectrophotometricallyMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetAdenosine receptor A1(Rattus norvegicus (rat))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50144902(3-(4-Hydroxy-phenyl)-2-methoxy-acrylic acid (3S,5R...)copy SMILEScopy InChI
Affinity DataIC50: 2.30E+4nMAssay Description:Displacement of [3H]DPCPX from adenosine A1 receptor of rat cortical membranes without GTPMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2VQ33FTPubMed
TargetAromatase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50298230(CHEMBL586557 | Monodictyochromone A)copy SMILEScopy InChI
Affinity DataIC50: 2.44E+4nMAssay Description:Inhibition of human recombinant aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2X34XHFPubMed
TargetAromatase(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50204912((1S,3S,4S,4aS,9aS)-1,4,8-trihydroxy-6-methoxy-3,4a...)copy SMILEScopy InChI
Affinity DataIC50: 2.83E+4nMAssay Description:Inhibition of human recombinant aromataseMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
TargetQuinone oxidoreductase(Mus musculus)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50204916(8-hydroxy-3-methyl-9-oxo-9H-xanthene-1-carboxylic ...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Induction of NAD(P)H:quinone reductase in mouse Hepa 1c1c7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
TargetQuinone oxidoreductase(Mus musculus)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50204913(2-(2,6-dihydroxybenzoyl)-3-hydroxy-5-methylbenzoic...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Induction of NAD(P)H:quinone reductase in mouse Hepa 1c1c7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
TargetQuinone oxidoreductase(Mus musculus)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50204915((1S,3S,4S,4aS,9aS)-1,4,8-trihydroxy-3,4a-dimethyl-...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Induction of NAD(P)H:quinone reductase in mouse Hepa 1c1c7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355307(CHEMBL1835012)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355305(CHEMBL1835010)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetQuinone oxidoreductase(Mus musculus)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50204912((1S,3S,4S,4aS,9aS)-1,4,8-trihydroxy-6-methoxy-3,4a...)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Induction of NAD(P)H:quinone reductase in mouse Hepa 1c1c7 cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2930STQPubMed
TargetAcetylcholinesterase(Electrophorus electricus (Electric eel))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355306(CHEMBL1835011)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of electric eel AChEMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetPapain(Carica papaya)
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355307(CHEMBL1835012)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of Carica papaya papainMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
TargetProthrombin(Homo sapiens (Human))
University of Bonn

Curated by ChEMBL
LigandPNGBDBM50355305(CHEMBL1835010)copy SMILEScopy InChI
Affinity DataIC50: 5.00E+4nMAssay Description:Inhibition of human thrombinMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2ZW1M94PubMed
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